Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Emily Mainetti"'
Autor:
Cristina Lucena-Serrano, Rafael Contreras-Cáceres, Manuel Lopez-Romero, Emily Mainetti, María Sánchez-Molina, Jean Manuel Cloarec, Miguel Angel Casado-Rodriguez
Publikováno v:
Current Organic Chemistry. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b23078f76d7c63c310c38d4ad3b8b32d
https://doi.org/10.2174/1385272821666161107160143
https://doi.org/10.2174/1385272821666161107160143
Autor:
Emily Mainetti, Juan Manuel Lopez Romero, Max Malacria, Kevin Cariou, Louis Fensterbank, Jean-Philippe Goddard, Malika Makhlouf, Stéphane Azzaro, Vincent Gandon, Youssef Harrak
Publikováno v:
Journal of Organometallic Chemistry. 696:388-399
The gold-catalyzed cycloisomerization of enynyl esters bearing a cyclohexyl template has been studied and has been shown to lead to two types of products arising from 1,2- vs. 1,3-O-acyl-migration. Results have shown to be dependent on the nature of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60ada788b738f3d9dc625c00893a72e6
https://doi.org/10.1016/j.jorganchem.2010.10.016
https://doi.org/10.1016/j.jorganchem.2010.10.016
Autor:
Shazia Anjum, Nicolas Marion, José Marco-Contelles, Louis Fensterbank, Gilles Lemière, Emily Mainetti, Virginie Mouries, Nieves Arroyo, Kevin Cariou, Max Malacria
Publikováno v:
European Journal of Organic Chemistry. 2006:4618-4633
The PtCl2- and PtCl4-catalyzed cycloisomerization of polyunsaturated precursors with different O-protecting groups at the propargylic position is reported. The free hydroxy, O-(bromomethyl)dimethylsilyl, O-methyl and O-propenyl derivatives 1a–f hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb9c44584ed66e88bbe5db98cdd33151
https://doi.org/10.1002/ejoc.200600521
https://doi.org/10.1002/ejoc.200600521
Publikováno v:
Tetrahedron. 60:9745-9755
1,6 Enyne systems flanked with an acetate group at the propargyl position undergo tandem PtCl 2 -catalyzed–thermal [3,3] rearrangements leading to trienes. The scope of the transformation has been delineated by varying the nature of the alkynyl sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e23ac81a1116474c2908683510b1c2b
https://doi.org/10.1016/j.tet.2004.06.151
https://doi.org/10.1016/j.tet.2004.06.151
Publikováno v:
European Journal of Organic Chemistry. 2003:1759-1764
We report the triphenyltin-mediated free-radical cyclization of 4-ethynyl-2,6,6-trimethylocta-1,7-dien-4-ol (1) and 4-ethynyl-6,6-dimethylocta-1,7-dien-4-ol (2), along with some chemical manipulations of the resulting stannylidene derivatives 3 and 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ce9de5b21e3c010ff12e6948bb5b0a0
https://doi.org/10.1002/ejoc.200310007
https://doi.org/10.1002/ejoc.200310007
Autor:
José Marco-Contelles, Juliana Ruiz-Caro, Emily Mainetti, Max Malacria, Louis Fensterbank, Priscille Devin
Publikováno v:
Tetrahedron. 58:1147-1158
The intramolecular Pauson–Khand (PK) reaction of 4-bromomethyldimethylsilyloxy-4-ethynyl-6,6-dimethyloct-1-en-7-yne ( 1 ), the differently functionalized 4-ethynyl-octa-1,7-dienes ( 2–6 ), and 5-ethynyl-5-hydroxy-2,4,4-trimethyl-nona-1,8-diene (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::712641aa7071899fe50c49bd7075fa31
https://doi.org/10.1016/s0040-4020(01)01209-1
https://doi.org/10.1016/s0040-4020(01)01209-1
Publikováno v:
Synlett. 2002:0923-0926
The reactivity of the α-cyclopropyl vinyl radical has been examined through the use of propargylic bromomethyldimethylsilyl ethers bearing a cyclopropyl group on the acetylenic moiety. With unsubstituted precursors, allenes can be obtained. With app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20ec1e76e32c1bd000eb60ecd5b0b15f
https://doi.org/10.1055/s-2002-31915
https://doi.org/10.1055/s-2002-31915
Publikováno v:
ChemInform. 33
The reactivity of the α-cyclopropyl vinyl radical has been examined through the use of propargylic bromomethyldimethylsilyl ethers bearing a cyclopropyl group on the acetylenic moiety. With unsubstituted precursors, allenes can be obtained. With app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9df59307cf9af2e82de88442a3bc602d
https://doi.org/10.1002/chin.200239070
https://doi.org/10.1002/chin.200239070
Publikováno v:
Synlett. 2000:1342-1344
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a50a46cf3f5755b79b08d950f6d710f
https://doi.org/10.1055/s-2000-7139
https://doi.org/10.1055/s-2000-7139
Publikováno v:
Angewandte Chemie (International ed. in English). 41(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b01b5a1b0da764b7f1d9576d9f74c6ed
https://pubmed.ncbi.nlm.nih.gov/19746619
https://pubmed.ncbi.nlm.nih.gov/19746619